9149
13549
ENSG00000105204ENSG00000281320
ENSMUSG00000002409
Q9Y463
Q9Z188
NM_004714NM_006483NM_006484
NM_001037957NM_001271370NM_010092
NP_004705NP_006474NP_006475NP_004705.1
NP_001033046NP_001258299NP_034222
Dual specificity tyrosine-phosphorylation-regulated kinase 1B is an enzyme that in humans is encoded by the DYRK1B gene.[5][6]
DYRK1B is a member of the DYRK family of protein kinases. DYRK1B contains a bipartite nuclear localization signal and is found mainly in muscle and testis. The protein is proposed to be involved in the regulation of nuclear functions. Three isoforms of DYRK1B have been identified differing in the presence of two alternatively spliced exons within the catalytic domain.[6]
DYRK1B has been shown to interact with:
One lone missense mutation in Dyrk1B gene (R102C) was found associated with an autosomal dominant early onset Coronary Artery Disease, juvenile-onset truncal obesity, severe hypertension, and type II diabetes mellitus - seen in subjects from a nomadic group in Iran.[9]
This article on a gene on human chromosome 19 is a stub. You can help Wikipedia by expanding it.
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